重新调整用途
胶质母细胞瘤
重编程
药物重新定位
药品
药理学
体外
医学
癌症研究
生物
细胞
生态学
生物化学
遗传学
作者
Qiyu Cao,Annika Hajosch,Richard E. Kast,Christopher Loehmann,Michal Hlaváč,Pamela Fischer‐Posovszky,Hannah A. Strobel,Mike‐Andrew Westhoff,Markus D. Siegelin,Christian Rainer Wirtz,Marc‐Eric Halatsch,Georg Karpel‐Massler
标识
DOI:10.1038/s41416-024-02608-8
摘要
Abstract Background Glioblastoma represents a brain tumor with a notoriously poor prognosis. First-line therapy may include adjunctive Tumor Treating Fields (TTFields) which are electric fields that are continuously delivered to the brain through non-invasive arrays. On a different note, CUSP9v3 represents a drug repurposing strategy that includes 9 repurposed drugs plus metronomic temozolomide. Here, we examined whether TTFields enhance the antineoplastic activity of CUSP9v3 against this disease. Methods We performed preclinical testing of a multimodal approach of TTFields and CUSP9v3 in different glioblastoma models. Results TTFields had predominantly synergistic inhibitory effects on the cell viability of glioblastoma cells and non-directed movement was significantly impaired when combined with CUSP9v3. TTFields plus CUSP9v3 significantly enhanced apoptosis, which was associated with a decreased mitochondrial outer membrane potential (MOMP), enhanced cleavage of effector caspase 3 and reduced expression of Bcl-2 and Mcl-1. Moreover, oxidative phosphorylation and expression of respiratory chain complexes I, III and IV was markedly reduced. Conclusion TTFields strongly enhance the CUSP9v3-mediated anti-glioblastoma activity. TTFields are currently widely used for the treatment of glioblastoma patients and CUSP9v3 was shown to have a favorable safety profile in a phase Ib/IIa trial (NCT02770378) which facilitates transition of this multimodal approach to the clinical setting.
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